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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252721Generated: October 28, 2026

Trimethylsilyl isocyanate → HCID 86620397, compound

https://huagongshe.com/reaction/252721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantHCID 86620393HCID 86620393—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86620397HCID 86620397—

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of trimethylsilyl isocyanate (0.032 mL), N-[5-(2-amino-4-methyl-1,3-thiazol-5-yl)-2-chloropyridin-3-yl]-2,4-dimethylthiazole-5-sulfonamide (46 mg) and DME (1 mL) was placed in a sealed glass reaction vessel and heated to 115° C. in a microwave reactor for 18 hours. The resultant mixture was evaporated and the residue was purified by preparative HPLC on reversed-phase silica using a solvent gradient of 10% to 100% acetonitrile in water (containing 1% acetic acid) as eluent. The material so obtained was triturated under diethyl ether. There was thus obtained the title compound as a solid (16 mg); 1H NMR Spectrum: (DMSOd6) 2.28 (s, 3H), 2.34 (s, 3H), 2.62 (s, 3H), 6.47 (br s, 2H), 7.71 (s, 1H), 8.34 (br s, 1H), 10.55 (s, 1H), 10:85 (br s, 1H); Mass Spectrum: M+H+ 459.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-cf1ee4ec7e5448db9127aa8f7f434aa6
Source noteuspto-grants-2011_01